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Early transcriptional events during osteogenic differentiation of human bone marrow stromal cells induced by Lim mineralization protein 3.

机译:Lim矿化蛋白3诱导人骨髓基质细胞成骨分化过程中的早期转录事件。

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摘要

Lim mineralization protein-3 (LMP3) induces osteoblast differentiation by regulating the expression and activity of certain molecules involved in the osteogenic cascade, including those belonging to the bone morphogenetic protein (BMP) family. The complete network of molecular events involved in LMP3-mediated osteogenesis is still unknown. The aim of this study was to analyze the genome-wide gene expression profiles in human mesenchymal stem cells (hMSC) induced by exogenous LMP3 to mediate osteogenesis. For this purpose hMSC were transduced with a defective adenoviral vector expressing the human LMP3 gene and microarray analysis was performed 1 day post-adenoviral transduction. Cells transduced with the vector backbone and untransduced cells were used as independent controls in the experiments. Microarray data were independently validated by means of real-time PCR on selected transcripts. The statistical analysis of microarray data produced a list of 263 significantly (p < 0.01) differentially expressed transcripts. The biological interpretation of the results indicated, among the most noteworthy effects, the modulation of genes involved in the TGF-beta1 pathway: 88 genes coding for key regulators of the cell cycle regulatory machinery and 28 genes implicated in the regulation of cell proliferation along with the development of connective, muscular, and skeletal tissues. These results suggested that LMP3 could affect the fine balance between cell proliferation/differentiation of mesenchymal cells mostly by modulating the TGF-beta1 signaling pathway.
机译:Lim矿化蛋白3(LMP3)通过调节参与成骨级联反应的某些分子(包括那些属于骨形态发生蛋白(BMP)家族的分子)的表达和活性来诱导成骨细胞分化。 LMP3介导的成骨过程涉及的分子事件的完整网络仍是未知的。这项研究的目的是分析外源性LMP3介导成骨作用的人间充质干细胞(hMSC)中的全基因组基因表达谱。为此目的,用表达人LMP3基因的有缺陷的腺病毒载体转导hMSC,并在腺病毒转导后1天进行微阵列分析。用载体主链转导的细胞和未转导的细胞在实验中用作独立对照。通过实时PCR对选定的转录本独立验证微阵列数据。微阵列数据的统计分析产生了263个显着(p <0.01)差异表达转录本的列表。结果的生物学解释表明,在最值得注意的作用中,涉及TGF-β1途径的基因的调制:88个基因编码细胞周期调控机制的关键调控因子,而28个基因与细胞增殖调控以及结缔组织,肌肉组织和骨骼组织的发育。这些结果表明,LMP3可能主要通过调节TGF-β1信号通路来影响间充质细胞增殖/分化之间的精细平衡。

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